List of variants in gene BRCC3 studied for Hereditary cancer-predisposing syndrome

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_001018055.3(BRCC3):c.493-404C>T	rs184669955	0.00667
NM_001018055.3(BRCC3):c.403+205A>G	rs190280980	0.00471
NM_001018055.3(BRCC3):c.403+3171G>A	rs376342905	0.00008
NM_001018055.3(BRCC3):c.123+84T>C	rs869312530	0.00007
NM_001018055.3(BRCC3):c.196-1496T>C	rs782283086	0.00006
NM_001018055.3(BRCC3):c.403+241A>G	rs869312528	0.00001
NM_001018055.3(BRCC3):c.403+3165C>A	rs869312527
NM_001018055.3(BRCC3):c.548+8153A>G	rs869312529

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